Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: snrpb2 ENSDARG00000039424

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Description

small nuclear ribonucleoprotein polypeptide B2 [Source:NCBI gene (formerly Entrezgene);Acc:402896]

Location

Chromosome 1: 51,702,087-51,710,340 reverse strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants), 263 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000057601.6	snrpb2-201	1124	220aa	ENSDARP00000057600.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	R4GDR2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSDART00000152745.2	snrpb2-202	1045	220aa	ENSDARP00000126617.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	R4GDR2	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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